2026· [Rinsho ketsueki] The Japanese journal of clinical hematology· Vol 67 8, pp.
902-909
· 0 citations
Medicine
TL;DR
This case underscores that, even in FV deficiency with a negative inhibitor screen, testing for anti-FV IgG is essential for identifying hyperclearance-type autoimmune FV deficiency (AiFVD), and ex vivo VET and TGT provided actionable assessments of hemostatic capacity and proved useful for guiding management in AiFVD.
Congenital Factor VII (FVII) deficiency is a rare inherited bleeding disorder characterized by
marked variability in bleeding severity and poor correlation between factor activity levels and
clinical phenotype. We report a 21-year-old woman who presented with recurrent spontaneous
ecchymoses without mucosal bleeding, m...
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Yuto Nakajima· International journal of hem...· 0 citations
Constitutional factor XIII deficiency is a rare inherited coagulation disorder, with an estimated worldwide prevalence of approximately 1 case per 2 million individuals. It is transmitted in an autosomal recessive pattern, and homozygous or compound heterozygous forms are associated with a characteristic bleeding pheno...
Kholoud Krimi, H. Mamad, Jalila Zirar et al.· Journal of Biology and Biome...· 0 citations
Preoperative screening tests are important for recognizing medical conditions that may mark surgical or anesthetic outcomes. This study evaluated the usefulness of routine coagulation screening in detecting bleeding risks prior to elective surgery. Over one year (January 2023–January 2024), 500 patients referred for pr...
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